Canonical Allele Identifier: CA5779214
Gene: HRAS HGNC NCBI
LRRC56 HGNC NCBI

Linked Data

ClinVar Variation Id: 415881
ClinVar RCV Id: RCV000465686
dbSNP Id: rs759004302
ExAC: 11:532687 A / C
gnomAD v2: 11-532687-A-C
gnomAD v4: 11-532687-A-C
MyVariant Identifiers: chr11:g.532687A>C (hg19) chr11:g.532687A>C (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.532687A>C , CM000673.2:g.532687A>C GRCh38
NC_000011.9:g.532687A>C , CM000673.1:g.532687A>C GRCh37
NC_000011.8:g.522687A>C NCBI36
NG_007666.1:g.7864T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000397594.7:c.*20-57T>G (HRAS) ENSP00000380722.3:n.*20-57T>G
ENST00000417302.7:c.*88T>G (HRAS) MANE Plus Clinical ENSP00000388246.1:n.*88T>G
ENST00000397594.6:c.251-57T>G (HRAS) ENSP00000380722.2:n.251-57T>G
ENST00000417302.6:c.*88T>G (HRAS) ENSP00000388246.1:n.*88T>G
ENST00000462734.2:c.*131T>G (HRAS) ENSP00000507303.1:n.*131T>G
ENST00000311189.8:c.519T>G (HRAS) MANE Select ENSP00000309845.7:p.Pro173=
ENST00000311189.7:c.519T>G (HRAS) ENSP00000309845.7:p.Pro173=
ENST00000397594.5:c.*88T>G (HRAS) ENSP00000380722.1:n.*88T>G
ENST00000397596.6:c.519T>G (HRAS) ENSP00000380723.2:p.Pro173=
ENST00000417302.5:c.*88T>G (HRAS) ENSP00000388246.1:n.*88T>G
ENST00000451590.5:c.519T>G (HRAS) ENSP00000407586.1:p.Pro173=
ENST00000462734.1:n.294T>G (HRAS)
ENST00000478324.5:n.243-57T>G (HRAS)
ENST00000479482.1:n.440T>G (HRAS)
ENST00000493230.5:c.*88T>G (HRAS) ENSP00000434023.1:n.*88T>G
NM_001130442.1:c.519T>G (HRAS) NP_001123914.1:p.Pro173=
NM_005343.2:c.519T>G (HRAS) NP_005334.1:p.Pro173=
NM_176795.3:c.*88T>G (HRAS) NP_789765.1:n.*88T>G
XM_011519875.1:c.-425+4350A>C (LRRC56) XP_011518177.1:n.-425+4350A>C
XM_011519877.1:c.-162+4350A>C (LRRC56) XP_011518179.1:n.-162+4350A>C
XR_242795.1:n.800T>G (HRAS)
NM_001130442.2:c.519T>G (HRAS) NP_001123914.1:p.Pro173=
NM_001318054.1:c.282T>G (HRAS) NP_001304983.1:p.Pro94=
NM_005343.3:c.519T>G (HRAS) NP_005334.1:p.Pro173=
NM_176795.4:c.*88T>G (HRAS) NP_789765.1:n.*88T>G
XM_011519875.2:c.-425+4350A>C (LRRC56) XP_011518177.1:n.-425+4350A>C
XM_011519877.2:c.-162+4350A>C (LRRC56) XP_011518179.1:n.-162+4350A>C
XM_017017167.1:c.-500+4350A>C (LRRC56) XP_016872656.1:n.-500+4350A>C
XM_017017168.1:c.-500+4350A>C (LRRC56) XP_016872657.1:n.-500+4350A>C
NM_005343.4:c.519T>G (HRAS) MANE Select NP_005334.1:p.Pro173=
NM_001318054.2:c.282T>G (HRAS) NP_001304983.1:p.Pro94=
NM_001130442.3:c.519T>G (HRAS) NP_001123914.1:p.Pro173=
NM_176795.5:c.*88T>G (HRAS) MANE Plus Clinical NP_789765.1:n.*88T>G
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